Canonical Allele Identifier: CA365376911

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390784A>C (hg19) ; chr6:g.112069581A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069581A>C , CM000668.2:g.112069581A>C	GRCh38
NC_000006.11:g.112390784A>C , CM000668.1:g.112390784A>C	GRCh37
NC_000006.10:g.112497477A>C	NCBI36
NG_011748.1:g.20507A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1026A>C MANE Select	ENSP00000357655.4:p.Arg342Ser
ENST00000639360.1:c.927A>C	ENSP00000491774.1:p.Arg309Ser
ENST00000230529.9:c.1026A>C	ENSP00000230529.5:p.Arg342Ser
ENST00000361714.5:c.1026A>C	ENSP00000354734.2:p.Arg342Ser
ENST00000368663.4:c.*332A>C	ENSP00000357652.4:n.*332A>C
ENST00000368664.7:c.*430A>C	ENSP00000357653.3:n.*430A>C
ENST00000368666.6:c.1080A>C	ENSP00000357655.3:p.Arg360Ser
ENST00000409166.5:c.354A>C	ENSP00000386467.1:p.Arg118Ser
ENST00000454589.5:c.*430A>C	ENSP00000395928.1:n.*430A>C
ENST00000604763.5:c.1026A>C	ENSP00000473777.1:p.Arg342Ser
ENST00000613648.1:n.861A>C
ENST00000620524.3:n.957A>C
NM_003880.3:c.1026A>C	NP_003871.1:p.Arg342Ser
NM_198239.1:c.1080A>C	NP_937882.1:p.Arg360Ser
NR_125353.1:n.1280A>C
NR_125354.1:n.1200A>C
XM_011536220.1:c.1026A>C	XP_011534522.1:p.Arg342Ser
XM_011536221.1:c.*430A>C	XP_011534523.1:n.*430A>C
XM_011536223.1:c.444A>C	XP_011534525.1:p.Arg148Ser
XM_011536223.3:c.444A>C	XP_011534525.1:p.Arg148Ser
XR_001743705.1:n.1628A>C
NM_003880.4:c.1026A>C	NP_003871.1:p.Arg342Ser
NM_198239.2:c.1026A>C MANE Select	NP_937882.2:p.Arg342Ser
NR_125353.2:n.1344A>C
NR_125354.3:n.1171A>C